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hydroxyindoleacetic acid and Dystonia

hydroxyindoleacetic acid has been researched along with Dystonia in 20 studies

(5-hydroxyindol-3-yl)acetic acid : A member of the class of indole-3-acetic acids that is indole-3-acetic acid substituted by a hydroxy group at C-5.

Dystonia: An attitude or posture due to the co-contraction of agonists and antagonist muscles in one region of the body. It most often affects the large axial muscles of the trunk and limb girdles. Conditions which feature persistent or recurrent episodes of dystonia as a primary manifestation of disease are referred to as DYSTONIC DISORDERS. (Adams et al., Principles of Neurology, 6th ed, p77)

Research Excerpts

ExcerptRelevanceReference
"Rapid-onset dystonia-parkinsonism (RDP) is characterized by sudden onset over hours to days of dystonia, dysphagia, dysarthria, and parkinsonism."5.30Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonism. ( Brashear, A; Butler, IJ; Dobyns, WB; Farlow, MR; Hyland, K, 1998)
"Two cases of severe dystonia and dyskinesia were treated with talipexole, a dopamine autoreceptor agonist, and the metabolites of dopamine, norepinephrine, and serotonin in cerebrospinal fluid (CSF) were determined."3.68Chronic treatment with talipexole dihydrochloride on abnormal involuntary movement in humans. ( Koga, I; Nishikawa, T; Tanaka, M; Tsuda, A; Uchida, Y; Yamada, S, 1990)
"Two pairs of siblings with severe dystonia with marked diurnal fluctuation had both reduced CSF concentration of biopterin and marked symptomatic improvement of the dystonia in response to levodopa."3.67Dystonia with marked diurnal variation associated with biopterin deficiency. ( Barton, N; Burns, RS; Cohen, W; Fink, JK; Hallett, M; Lovenberg, W, 1988)
"Homovanillic acid (HVA) and 5-hydroxyindoleacetic acid (5-HIAA), the respective metabolites of dopamine and serotonin, were measured in ventricular fluid obtained from 20 patients with torsion dystonia at the time of ventriculography prior to thalamic surgery."3.66Diminished ventricular fluid dopamine metabolites in adult-onset dystonia. ( Sharpless, NS; Tabaddor, K; Wolfson, LI, 1978)
"Mitochondrial disorders are clinically heterogeneous."1.35Mitochondrial diseases mimicking neurotransmitter defects. ( Artuch, R; Briones, P; Carrilho, I; Duarte, S; Garcia-Cazorla, A; Garesse, R; Montoya, J; Nascimento, A; Ormazabal, A; Pineda, M; Sala-Castellvi, P; Serrano, M, 2008)
"The typical infantile form of dystonia is benign, resolving by 2 years of age in an otherwise normal child."1.31Infantile-onset paroxysmal dystonia: a diagnostic dilemma. ( Antony, J; Howman-Giles, R; Wilmshurst, JM, 2001)
"Childhood dystonia that does not respond to treatment with levodopa (dopa-nonresponsive dystonia, DND) has an unclear pathogenesis and is notoriously difficult to treat."1.31Selective decrease in central nervous system serotonin turnover in children with dopa-nonresponsive dystonia. ( Assmann, B; Heales, S; Hoffmann, GF; Köhler, M; Surtees, R, 2002)
"Rapid-onset dystonia-parkinsonism (RDP) is characterized by sudden onset over hours to days of dystonia, dysphagia, dysarthria, and parkinsonism."1.30Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonism. ( Brashear, A; Butler, IJ; Dobyns, WB; Farlow, MR; Hyland, K, 1998)
"Rapid-onset dystonia-parkinsonism (RDP) is an autosomal dominant disorder characterized by the rapid onset of dystonic spasms and parkinsonism over a period of a few hours to weeks after their onset."1.29Variable phenotype of rapid-onset dystonia-parkinsonism. ( Brashear, A; Butler, IJ; Dobyns, WB; Farlow, MR; Kasarskis, EJ, 1996)
"HVA levels in dystonia patients (30."1.29Neurotransmitters in CSF of idiopathic adult-onset dystonia: reduced 5-HIAA levels as evidence of impaired serotonergic metabolism. ( Götz, M; Lange, KW; Naumann, M; Reiners, K; Riederer, P, 1996)
"We describe two sporadic cases of dystonia-parkinsonism at different stages of disease progression."1.28Consideration on two cases of dystonia-parkinsonism. ( Balottin, U; Borgatti, R; Lanzi, G; Zambrino, CA, 1991)

Research

Studies (20)

TimeframeStudies, this research(%)All Research%
pre-19909 (45.00)18.7374
1990's6 (30.00)18.2507
2000's4 (20.00)29.6817
2010's1 (5.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Garcia-Cazorla, A1
Duarte, S1
Serrano, M1
Nascimento, A1
Ormazabal, A1
Carrilho, I1
Briones, P1
Montoya, J1
Garesse, R1
Sala-Castellvi, P1
Pineda, M1
Artuch, R1
Kurian, MA1
Li, Y1
Zhen, J1
Meyer, E1
Hai, N1
Christen, HJ1
Hoffmann, GF2
Jardine, P1
von Moers, A1
Mordekar, SR1
O'Callaghan, F1
Wassmer, E1
Wraige, E1
Dietrich, C1
Lewis, T1
Hyland, K2
Heales, S2
Sanger, T1
Gissen, P1
Assmann, BE1
Reith, ME1
Maher, ER1
Barnett, MH1
Jarman, PR1
Heales, SJ1
Bhatia, KP1
Willemse, J1
van Nieuwenhuizen, O1
Gooskens, RH1
Westenberg, HG1
Ledoux, MS1
Lorden, JF1
Ervin, JM1
Brashear, A2
Farlow, MR2
Butler, IJ2
Kasarskis, EJ1
Dobyns, WB2
Naumann, M1
Götz, M1
Reiners, K1
Lange, KW1
Riederer, P1
Wilmshurst, JM1
Howman-Giles, R1
Antony, J1
Assmann, B1
Köhler, M1
Surtees, R1
Tabaddor, K1
Wolfson, LI2
Sharpless, NS2
Ouvrier, RA1
Nishikawa, T1
Yamada, S1
Tsuda, A1
Tanaka, M1
Koga, I1
Uchida, Y1
Zambrino, CA1
Balottin, U1
Borgatti, R1
Lanzi, G1
Fink, JK2
Barton, N1
Cohen, W1
Lovenberg, W2
Burns, RS2
Hallett, M2
Thal, LJ1
LeWitt, PA1
Miller, LP1
Levine, RA2
Newman, RP1
Papavasiliou, A1
Rayes, A1
Eldridge, R1
Maekawa, N1
Hashimoto, T1
Sasaki, M1
Oishi, T1
Tsuji, S1
Ravin, P1
Argoff, CE1
Brady, RO1
Barton, NW1
Stahl, SM1
Faull, KF1
Barchas, JD1
Berger, PA1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Cerebral Autoregulation in Patients With Aneurysmal SubArachnoid Haemorrhage[NCT03987139]45 participants (Anticipated)Interventional2019-06-15Active, not recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Other Studies

20 other studies available for hydroxyindoleacetic acid and Dystonia

ArticleYear
Mitochondrial diseases mimicking neurotransmitter defects.
    Mitochondrion, 2008, Volume: 8, Issue:3

    Topics: Alanine; Brain; Child, Preschool; Consanguinity; Diagnosis, Differential; Dopamine Agents; Dystonia;

2008
Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study.
    The Lancet. Neurology, 2011, Volume: 10, Issue:1

    Topics: Brain; Cell Line, Transformed; Child; Child, Preschool; Cohort Studies; Dopamine Plasma Membrane Tra

2011
Further case of paroxysmal exercise-induced dystonia and some insights into pathogenesis.
    Movement disorders : official journal of the Movement Disorder Society, 2002, Volume: 17, Issue:6

    Topics: Adult; Dopamine; Dystonia; Exercise; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Male; Neur

2002
Treatment of non-fluctuating progressive dystonia: a neuropharmacological approach.
    Neuropediatrics, 1984, Volume: 15, Issue:4

    Topics: Adolescent; Basal Ganglia; Child; Chromatography, High Pressure Liquid; Dystonia; Female; Homovanill

1984
Inferior olive serotonin and norepinephrine levels during development in the genetically dystonic rat.
    Brain research bulletin, 1994, Volume: 33, Issue:3

    Topics: Aging; Animals; Animals, Newborn; Chromatography, High Pressure Liquid; Dystonia; Hydroxyindoleaceti

1994
Variable phenotype of rapid-onset dystonia-parkinsonism.
    Movement disorders : official journal of the Movement Disorder Society, 1996, Volume: 11, Issue:2

    Topics: Adolescent; Adult; Dopamine; Dystonia; Female; Follow-Up Studies; Genetic Carrier Screening; Homovan

1996
Neurotransmitters in CSF of idiopathic adult-onset dystonia: reduced 5-HIAA levels as evidence of impaired serotonergic metabolism.
    Journal of neural transmission (Vienna, Austria : 1996), 1996, Volume: 103, Issue:8-9

    Topics: Adult; Age of Onset; Aged; Aged, 80 and over; Case-Control Studies; Dopamine; Dystonia; Female; Homo

1996
Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonism.
    Annals of neurology, 1998, Volume: 43, Issue:4

    Topics: Adult; Aged; Antiparkinson Agents; Biomarkers; Deglutition Disorders; Dopamine; Dysarthria; Dystonia

1998
Infantile-onset paroxysmal dystonia: a diagnostic dilemma.
    Journal of child neurology, 2001, Volume: 16, Issue:3

    Topics: Brain; Consanguinity; Dominance, Cerebral; Dystonia; Homovanillic Acid; Humans; Hydroxyindoleacetic

2001
Selective decrease in central nervous system serotonin turnover in children with dopa-nonresponsive dystonia.
    Pediatric research, 2002, Volume: 52, Issue:1

    Topics: Adolescent; Central Nervous System; Child; Child, Preschool; Dihydroxyphenylalanine; Dopamine Agents

2002
Diminished ventricular fluid dopamine metabolites in adult-onset dystonia.
    Neurology, 1978, Volume: 28, Issue:12

    Topics: Adolescent; Adult; Age Factors; Child; Child, Preschool; Dystonia; Female; Homovanillic Acid; Humans

1978
Progressive dystonia with marked diurnal fluctuation.
    Annals of neurology, 1978, Volume: 4, Issue:5

    Topics: Child; Circadian Rhythm; Diagnosis, Differential; Dystonia; Female; Homovanillic Acid; Humans; Hydro

1978
Chronic treatment with talipexole dihydrochloride on abnormal involuntary movement in humans.
    Clinical neuropharmacology, 1990, Volume: 13, Issue:3

    Topics: 3,4-Dihydroxyphenylacetic Acid; Aged; Azepines; Dopamine Agents; Dystonia; Homovanillic Acid; Humans

1990
Consideration on two cases of dystonia-parkinsonism.
    Italian journal of neurological sciences, 1991, Volume: 12, Issue:5

    Topics: Carbidopa; Child; Dystonia; Female; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Levodopa; M

1991
Dystonia with marked diurnal variation associated with biopterin deficiency.
    Neurology, 1988, Volume: 38, Issue:5

    Topics: Adolescent; Adult; Biopterins; Carbidopa; Child; Child, Preschool; Circadian Rhythm; Drug Combinatio

1988
Diminished levels of ventricular fluid norepinephrine metabolite and somatostatin in childhood-onset dystonia.
    Advances in neurology, 1988, Volume: 50

    Topics: Adolescent; Adult; Age Factors; Cerebral Palsy; Child; Child, Preschool; Dystonia; Homovanillic Acid

1988
Pterin abnormalities in dystonia: a metabolic marker with therapeutic implications.
    Advances in neurology, 1988, Volume: 50

    Topics: Adult; Biopterins; Central Nervous System; Dystonia; Homovanillic Acid; Humans; Hydroxyindoleacetic

1988
[A study on catecholamine metabolites in CSF in a patient with progressive dystonia with marked diurnal fluctuation].
    Rinsho shinkeigaku = Clinical neurology, 1988, Volume: 28, Issue:10

    Topics: Adolescent; Catecholamines; Circadian Rhythm; Dystonia; Female; Homovanillic Acid; Humans; Hydroxyin

1988
Tetrahydrobiopterin administration in biopterin-deficient progressive dystonia with diurnal variation.
    Neurology, 1989, Volume: 39, Issue:10

    Topics: Adult; Biopterins; Child; Circadian Rhythm; Dystonia; Female; Homovanillic Acid; Humans; Hydroxyindo

1989
CSF monamine metabolites in movement disorders and normal aging.
    Archives of neurology, 1985, Volume: 42, Issue:2

    Topics: 3,4-Dihydroxyphenylacetic Acid; Adult; Aged; Dyskinesia, Drug-Induced; Dystonia; Female; Glycols; Ho

1985